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Page 1
Clinical Features of Machado-Joseph Disease.
Mendonça N, França MC Jr, Gonçalves AF, Januário C. Mendonça N, et al. Among authors: januario c. Adv Exp Med Biol. 2018;1049:255-273. doi: 10.1007/978-3-319-71779-1_13. Adv Exp Med Biol. 2018. PMID: 29427108 Review.
Protocol for the Characterization of the Cytosine-Adenine-Guanine Tract and Flanking Polymorphisms in Machado-Joseph Disease: Impact on Diagnosis and Development of Gene-Based Therapies.
Lopes SM, Faro R, Lopes MM, Onofre I, Mendonça N, Ribeiro J, Januário C, Nobre RJ, Pereira de Almeida L. Lopes SM, et al. Among authors: januario c. J Mol Diagn. 2020 Jun;22(6):782-793. doi: 10.1016/j.jmoldx.2020.03.003. Epub 2020 Mar 20. J Mol Diagn. 2020. PMID: 32205289 Free article.
Cerebellar morphometric and spectroscopic biomarkers for Machado-Joseph Disease.
Miranda CO, Nobre RJ, Paiva VH, Duarte JV, Castelhano J, Petrella LI, Sereno J, Santana M, Afonso S, Januário C, Castelo-Branco M, de Almeida LP. Miranda CO, et al. Among authors: januario c. Acta Neuropathol Commun. 2022 Mar 19;10(1):37. doi: 10.1186/s40478-022-01329-4. Acta Neuropathol Commun. 2022. PMID: 35305685 Free PMC article.
Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity.
Hengel H, Martus P, Faber J, Garcia-Moreno H, Solanky N, Giunti P, Klockgether T, Reetz K, van de Warrenburg BP, Pereira de Almeida L, Santana MM, Januário C, Silva P, Thieme A, Infante J, de Vries J, Lima M, Ferreira AF, Bushara K, Jacobi H, Onyike C, Schmahmann JD, Hübener-Schmid J, Synofzik M, Schöls L. Hengel H, et al. Among authors: januario c. Mov Disord. 2022 Feb;37(2):405-410. doi: 10.1002/mds.28844. Epub 2021 Oct 29. Mov Disord. 2022. PMID: 34713931
Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3.
Prudencio M, Garcia-Moreno H, Jansen-West KR, Al-Shaikh RH, Gendron TF, Heckman MG, Spiegel MR, Carlomagno Y, Daughrity LM, Song Y, Dunmore JA, Byron N, Oskarsson B, Nicholson KA, Staff NP, Gorcenco S, Puschmann A, Lemos J, Januário C, LeDoux MS, Friedman JH, Polke J, Labrum R, Shakkottai V, McLoughlin HS, Paulson HL, Konno T, Onodera O, Ikeuchi T, Tada M, Kakita A, Fryer JD, Karremo C, Gomes I, Caviness JN, Pittelkow MR, Aasly J, Pfeiffer RF, Veerappan V, Eggenberger ER, Freeman WD, Huang JF, Uitti RJ, Wierenga KJ, Marin Collazo IV, Tipton PW, van Gerpen JA, van Blitterswijk M, Bu G, Wszolek ZK, Giunti P, Petrucelli L. Prudencio M, et al. Among authors: januario c. Sci Transl Med. 2020 Oct 21;12(566):eabb7086. doi: 10.1126/scitranslmed.abb7086. Sci Transl Med. 2020. PMID: 33087504 Free PMC article.
Ubiquitin proteasome system in Parkinson's disease: a keeper or a witness?
Martins-Branco D, Esteves AR, Santos D, Arduino DM, Swerdlow RH, Oliveira CR, Januario C, Cardoso SM. Martins-Branco D, et al. Among authors: januario c. Exp Neurol. 2012 Dec;238(2):89-99. doi: 10.1016/j.expneurol.2012.08.008. Epub 2012 Aug 19. Exp Neurol. 2012. PMID: 22921536 Free PMC article.
Bioenergetic dysfunction in Huntington's disease human cybrids.
Ferreira IL, Cunha-Oliveira T, Nascimento MV, Ribeiro M, Proença MT, Januário C, Oliveira CR, Rego AC. Ferreira IL, et al. Among authors: januario c. Exp Neurol. 2011 Sep;231(1):127-34. doi: 10.1016/j.expneurol.2011.05.024. Epub 2011 Jun 13. Exp Neurol. 2011. PMID: 21684277
94 results